Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • drgoettel
    Junior Member
    • Jun 2009
    • 5

    #1

    Where is the read?

    Hello,

    I have "lost" one read in a 454 assembly. That read is in the .sff used to run the assembly.
    It's also at 454ReadStatus.txt file telling that it became a Singleton

    nameoftheread Singleton

    It also has been trimmed:
    Accno Trimpoints Used Used Trimmed Length Orig Trimpoints Orig Trimmed Length Raw Length
    nameoftheread 5-270 266 5-270 266 270

    I have the "allContigThresh" parameter to 100.

    So anybody knows why isn't this read at 454AllContigs.fna output??
    Where has it gone?

    Thanks in advance.






    PD: I write down the qualities extracted from the sff file, in case they can help:

    Bases: tcagTCGCAAGTGCCACGACCAGAAAGAATTGATGGTGGCGGTTGTTTGCCACACGACCTCTCCCGAAGACTTTGGAGGTAATGCCGACATTGGATCTGGCAAGAACAAAGCTTAACCCTAATTTATTTTATAGCAATAGCAAGGGTTAAGCTTTGTTCTTTCCATATTTGATGTCAGCATTCCCTCCTAAGACTCAGGAATGGATGTGGAAATTGTGCTTCGCAAGAACCTACAGTCGTCGCTTCGGTATGGACAAAGCTTGAAGGTTG
    Quality Scores: 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 33 20 20 23 23 22 22 31 31 33 33 35 35 35 35 35 35 36 35 35 35 35 35 35 35 35 35 31 31 31 33 35 35 35 35 33 33 33 35 35 31 31 31 33 33 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 33 33 33 35 35 35 35 35 35 35 35 35 35 35 35 33 31 31 31 33 35 35 35 35 31 31 31 35 35 31 31 31 31 17 17 17 25 24 24 25 25 25 31 20 20 20 20 35 35 35 35 33 31 31 32 35 35 35 30 30 21 21 21 21 21 33 33 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 33 33 33 35 35 35 35 35 35 35 35 35 35 35 35 33 33 33 35 35 35 35 35 35 35 35 35 35 35 35 35 35 33 33 33 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 35 33 31 31 33 34 34 34 34 34 34 27 27 27 33 34 34 34 34 34 34 34 34 34 34 31 31 31 26 26 26 28 28 28 28 29 28 28 28 28 28 28 28 28 28 22 22 22 22 22 22 22
  • kmcarr
    Senior Member
    • May 2008
    • 1181

    #2
    The answer is there in the 454ReadStatus.txt file. This read is a "Singleton" meaning it was not assembled into any contig, that's why it's not in the 454AllContigs.fna. That file does not include singletons.

    If your assembly is typical you should have many more than just one Singleton remaining. Look at the readStatus section of your 454NewblerMetrics.txt file to see the total of Assembled, Singleton, et al. in your assembly.

    If you want to recover a file of the unassembled (Singleton) reads you could create a text file listing their IDs (taken from the ReadStatus file) and use this list in conjunction with the sfffile and sffinfo tools to extract the singleton reads from the sff file.
    Last edited by kmcarr; 02-14-2011, 09:25 AM. Reason: Added sfffile to the programs needed to extract a subset of reads.

    Comment

    • drgoettel
      Junior Member
      • Jun 2009
      • 5

      #3
      numreads=1?

      Thankyou for your answer
      But inside 454AllContigs.fna are a lot of "contigs" with numreads=1
      They are singletons to me. Aren't they??

      Comment

      • kmcarr
        Senior Member
        • May 2008
        • 1181

        #4
        Originally posted by drgoettel View Post
        Thankyou for your answer
        But inside 454AllContigs.fna are a lot of "contigs" with numreads=1
        They are singletons to me. Aren't they??
        No, those are not classified as singletons. The read which makes up a single read contig will be listed as Assembled in the 454ReadStatus file.

        Now you may ask, how come some reads are singletons and other assembled as single read contigs? Not knowing the internals of the gsAssembler I can't answer definitively but my guess is that these single read contigs may have been been part of larger contigs originally but these reads were ripped out during latter stages of the assembly for whatever reason. They then become classified as single read contigs vs singletons which are reads which were never included in any contig. Again, this is only a guess.

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
          by SEQadmin2



          CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

          Despite this, “CRISPR helped turn genome editing from a specialized technique into
          ...
          07-31-2026, 11:01 AM
        • SEQadmin2
          Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
          by SEQadmin2


          Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

          The systematic characterization of the human proteome has
          ...
          07-20-2026, 11:48 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 10:05 AM
        0 responses
        8 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-13-2026, 12:22 PM
        0 responses
        33 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-11-2026, 10:35 AM
        0 responses
        27 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-06-2026, 07:41 AM
        0 responses
        38 views
        0 reactions
        Last Post SEQadmin2  
        Working...